Search Database

Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
Q14126 DSG2 Desmoglein-2 (Cadherin family member 5) … Homo sapiens (Human) 1118 aa

Protein Details: Q14126 (DSG2)

Protein Information
AccessionQ14126
Protein NamesDesmoglein-2 (Cadherin family member 5) (HDGC)
Gene SymbolDSG2
OrganismHomo sapiens (Human)
Length1118 aa
IsoformsNo isoforms
Related PMIDs 26111759 29575903 29733200 31251020 33636221 31251020 (mass) 32651440 (mass) 36430497 (mass)
Database SourcesdbPTMSwissPalm
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Types:
Experimental Database High Prediction Non-palmitylated Cys
1-501MARSPGRAYA11LLLLLICFNV21GSGLHLQVLS31TRNENKLLPK41HPHLVRQKRA
51-10051WITAPVALRE61GEDLSKKNPI71AKIHSDLAEE81RGLKITYKYT91GKGITEPPFG
101-150101IFVFNKDTGE111LNVTSILDRE121ETPFFLLTGY131ALDARGNNVE141KPLELRIKVL
151-200151DINDNEPVFT161QDVFVGSVEE171LSAAHTLVMK181INATDADEPN191TLNSKISYRI
201-250201VSLEPAYPPV211FYLNKDTGEI221YTTSVTLDRE231EHSSYTLTVE241ARDGNGEVTD
251-300251KPVKQAQVQI261RILDVNDNIP271VVENKVLEGM281VEENQVNVEV291TRIKVFDADE
301-350301IGSDNWLANF311TFASGNEGGY321FHIETDAQTN331EGIVTLIKEV341DYEEMKNLDF
351-400351SVIVANKAAF361HKSIRSKYKP371TPIPIKVKVK381NVKEGIHFKS391SVISIYVSES
401-450401MDRSSKGQII411GNFQAFDEDT421GLPAHARYVK431LEDRDNWISV441DSVTSEIKLA
451-500451KLPDFESRYV461QNGTYTVKIV471AISEDYPRKT481ITGTVLINVE491DINDNCPTLI
501-550501EPVQTICHDA511EYVNVTAEDL521DGHPNSGPFS531FSVIDKPPGM541AEKWKIARQE
551-600551STSVLLQQSE561KKLGRSEIQF571LISDNQGFSC581PEKQVLTLTV591CECLHGSGCR
601-650601EAQHDSYVGL611GPAAIALMIL621AFLLLLLVPL631LLLMCHCGKG641AKGFTPIPGT
651-700651IEMLHPWNNE661GAPPEDKVVP671SFLPVDQGGS681LVGRNGVGGM691AKEATMKGSS
701-750701SASIVKGQHE711MSEMDGRWEE721HRSLLSGRAT731QFTGATGAIM741TTETTKTARA
751-800751TGASRDMAGA761QAAAVALNEE771FLRNYFTDKA781ASYTEEDENH791TAKDCLLVYS
801-850801QEETESLNAS811IGCCSFIEGE821LDDRFLDDLG831LKFKTLAEVC841LGQKIDINKE
851-900851IEQRQKPATE861TSMNTASHSL871CEQTMVNSEN881TYSSGSSFPV891PKSLQEANAE
901-950901KVTQEIVTER911SVSSRQAQKV921ATPLPDPMAS931RNVIATETSY941VTGSTMPPTT
951-1000951VILGPSQPQS961LIVTERVYAP971ASTLVDQPYA981NEGTVVVTER991VIQPHGGGSN
1001-10501001PLEGTQHLQD1011VPYVMVRERE1021SFLAPSSGVQ1031PTLAMPNIAV1041GQNVTVTERV
1051-11001051LAPASTLQSS1061YQIPTENSMT1071ARNTTVSGAG1081VPGPLPDFGL1091EESGHSNSTI
1101-11181101TTSSTRVTKH1111STVQHSYS
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
17 - - -
GPS-Palm: 0.66
Deep-Palm: 0.98
496 - - -
Deep-Palm: 0.06
507 - - -
Deep-Palm: 0.05
580 - - -
Deep-Palm: 0.53
591 - - -
Deep-Palm: 0.65
593 - - -
Deep-Palm: 0.43
599 - - -
Deep-Palm: 0.73
635 DBPTM SWISSPALM - - -
GPS-Palm: 0.94
Deep-Palm: 0.99
637 DBPTM SWISSPALM - - -
GPS-Palm: 0.87
Deep-Palm: 0.98
795 - - -
Deep-Palm: 0.63
813 - - -
Deep-Palm: 0.64
814 - - -
Deep-Palm: 0.77
840 - - -
GPS-Palm: 0.95
Deep-Palm: 0.98
871 - - -
Deep-Palm: 0.21
Score Interpretation:
GPS-Palm: Thresholds - High (≥0.8920), Medium (≥0.7766), Low (≥0.6484), Very Low (<0.6484)
Deep-Palm: Higher score indicates higher probability of palmitoylation (High ≥0.9)
Tissue/Cell Line Expression
Literature Data - Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 0.400
4
LNCaP
Specificity: 0.364
4/4 (100.0%)
2
HeLa cell
Specificity: 0.182
2/2 (100.0%)
2
Jurkat T cell
Specificity: 0.182
2/2 (100.0%)
1
HAP1 cell
Specificity: 0.091
1/1 (100.0%)
1
heart
Specificity: 0.091
1/1 (100.0%)
Mass Spectrometry Data - Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 1.000
1
LNCaP cells (Mass)
Specificity: 0.091
1/4 (25.0%)
Palmitoylation Distribution by Study and Tissue/Cell Line
Chart Explanation: Each bar represents a study (PMID). Blue bars: Literature data, Orange bars: Mass Spectrometry data. The colored bottom segment shows palmitoylated samples, while the gray top segment shows non-palmitoylated samples.
Conservation score for cysteine
PhyloP for Cysteine
PhastCons Conservation Scores for Cysteine
TCGA Cysteine Mutation Information

Note: Mutations indicate amino acid changes that may create potential palmitoylation sites.

Position Amino Acid Change Frequency Type Function Cancer Type
261 R → C 0.002141 SNP Missense Mutation SKCM
635 C → W 0.002141 SNP Missense Mutation SKCM
635 C → Y 0.001887 SNP Missense Mutation UCEC
637 C → C 0.002294 SNP Silent OV
871 C → F 0.008130 SNP Missense Mutation THYM
960 S → C 0.001969 SNP Missense Mutation LGG